Abstract
Y-27632 and its enantiomer were synthesized in 8 steps from trans-1,4-cyclohexanedicarboxylic acid by using a diastereoselective reductive amination of a ketone.
Keywords: kinase inhibitor, rho-associated kinase, reductive amination
Letters in Organic Chemistry
Title: Short Synthesis of the Selective Rho-Kinase Inhibitor Y-27632 and of Its Enantiomer
Volume: 2 Issue: 7
Author(s): D. Belotti, J. L. Peglion and J. Cossy
Affiliation:
Keywords: kinase inhibitor, rho-associated kinase, reductive amination
Abstract: Y-27632 and its enantiomer were synthesized in 8 steps from trans-1,4-cyclohexanedicarboxylic acid by using a diastereoselective reductive amination of a ketone.
Export Options
About this article
Cite this article as:
Belotti D., Peglion L. J. and Cossy J., Short Synthesis of the Selective Rho-Kinase Inhibitor Y-27632 and of Its Enantiomer, Letters in Organic Chemistry 2005; 2 (7) . https://dx.doi.org/10.2174/157017805774297019
DOI https://dx.doi.org/10.2174/157017805774297019 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
- Author Guidelines
- Graphical Abstracts
- Fabricating and Stating False Information
- Research Misconduct
- Post Publication Discussions and Corrections
- Publishing Ethics and Rectitude
- Increase Visibility of Your Article
- Archiving Policies
- Peer Review Workflow
- Order Your Article Before Print
- Promote Your Article
- Manuscript Transfer Facility
- Editorial Policies
- Allegations from Whistleblowers